NDC11 21130060105
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 21130-0601-05 | 21130-0601 |
| 21130-0601-5 | 21130-0601 |
| 21130-601-05 | 21130-601 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Eye Itch Relief | KETOTIFEN FUMARATE | Safeway | 5fccbb63-7859-484c-b7b3-9de711364c09 | 2024-05-16 | Warnings | 21130-601-05 21130-601 21130060105 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.